JPH07123969A - Production of alcoholic drink - Google Patents

Production of alcoholic drink

Info

Publication number
JPH07123969A
JPH07123969A JP34706793A JP34706793A JPH07123969A JP H07123969 A JPH07123969 A JP H07123969A JP 34706793 A JP34706793 A JP 34706793A JP 34706793 A JP34706793 A JP 34706793A JP H07123969 A JPH07123969 A JP H07123969A
Authority
JP
Japan
Prior art keywords
reactor
yeast
culture
brewing
immobilized
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP34706793A
Other languages
Japanese (ja)
Other versions
JP3604715B2 (en
Inventor
Akira Shindo
昌 進藤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sapporo Breweries Ltd
Original Assignee
Sapporo Breweries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to JP34706793A priority Critical patent/JP3604715B2/en
Application filed by Sapporo Breweries Ltd filed Critical Sapporo Breweries Ltd
Priority to EP94926367A priority patent/EP0669393A4/en
Priority to AU76236/94A priority patent/AU674448B2/en
Priority to CA002147511A priority patent/CA2147511A1/en
Priority to US08/424,433 priority patent/US20010019731A1/en
Priority to PCT/JP1994/001476 priority patent/WO1995007343A1/en
Priority to KR1019950701752A priority patent/KR950704472A/en
Priority to CN94190661A priority patent/CN1068378C/en
Publication of JPH07123969A publication Critical patent/JPH07123969A/en
Application granted granted Critical
Publication of JP3604715B2 publication Critical patent/JP3604715B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12CBEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00Fermentation processes for beer
    • C12C11/07Continuous fermentation
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12CBEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00Fermentation processes for beer
    • C12C11/07Continuous fermentation
    • C12C11/075Bioreactors for continuous fermentation
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12CBEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00Fermentation processes for beer
    • C12C11/09Fermentation with immobilised yeast
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12GWINE; PREPARATION THEREOF; ALCOHOLIC BEVERAGES; PREPARATION OF ALCOHOLIC BEVERAGES NOT PROVIDED FOR IN SUBCLASSES C12C OR C12H
    • C12G1/00Preparation of wine or sparkling wine
    • C12G1/02Preparation of must from grapes; Must treatment and fermentation
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12GWINE; PREPARATION THEREOF; ALCOHOLIC BEVERAGES; PREPARATION OF ALCOHOLIC BEVERAGES NOT PROVIDED FOR IN SUBCLASSES C12C OR C12H
    • C12G3/00Preparation of other alcoholic beverages
    • C12G3/02Preparation of other alcoholic beverages by fermentation
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M25/00Means for supporting, enclosing or fixing the microorganisms, e.g. immunocoatings
    • C12M25/16Particles; Beads; Granular material; Encapsulation
    • C12M25/20Fluidized bed
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M29/00Means for introduction, extraction or recirculation of materials, e.g. pumps
    • C12M29/18External loop; Means for reintroduction of fermented biomass or liquid percolate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Microbiology (AREA)
  • Food Science & Technology (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Sustainable Development (AREA)
  • Mycology (AREA)
  • Immunology (AREA)
  • Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
  • Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Alcoholic Beverages (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

PURPOSE:To obtain an alcoholic drink reduced in amino acid concentration through such processes that a fluidized bed-type reactor having both fluid circulating pipe and exhaust vent is packed with an immobilized enzyme followed by feeding the 10 reactor with a brewing feedstock liquor and conducting a culture while drawing the culture fluid via the top of the reactor and returning it to the lower part of the reactor. CONSTITUTION:A fluidized bed-type reactor 4 equipped with a fluid circulating pipe, gas exhaust vent 6, thermosensor 5 and pH sensor 3, etc., is packed with an immobilized yeast with a beer yeast such as Saccharomyces cerevisiae IAM4206 (ATCC 9080) immobilized on a carrier like chitosan beads, and this reactor 4 is fed, from a malt juice tank 1, with a brewing feedstock liquor adjusted to 11wt.% in raw malt juice extract level through a pump 2, part of the culture fluid is drawn via the top of the reactor 4 and returned, via the lower part of the reactor, into the reactor 4, thus conducting a culture while forming a circulating flow and obtaining the objective drink with good flavor, reduced in amino acid concentration because most of the carbon dioxide produced can be discharged via the gas exhaust vent 6 out of the system and the amino acid in the brewing feedstock liquor can be assimilated efficiently.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、酒類の製造法に関し、
詳しくは発酵中に産生される炭酸ガスの排出を容易に
し、かつ酵母による原料中のアミノ酸の取り込みを促進
させ、香味の安定した酒類を速やかに製造する方法に関
する。
FIELD OF THE INVENTION The present invention relates to a method for producing alcoholic beverages,
More particularly, it relates to a method for facilitating the discharge of carbon dioxide gas produced during fermentation, promoting the uptake of amino acids in raw materials by yeast, and rapidly producing alcoholic beverages having a stable flavor.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】ビー
ル,ワイン等の酒類の製造工程では、一般に醸造原料液
中の炭素源,窒素源が酵母により消費されてエチルアル
コールが生成される。酵母を固定化する技術、例えば酵
母を含水ゲル中に包埋させて固定化する技術が開発され
てから、麦汁の連続醸造によるビールの製造法が提案さ
れている(J.Inst. Brew.,84,228(1981)。これらの方法
は、酵母を高濃度で使用できるため、醸造期間の大幅な
短縮が可能である。しかし、固定化酵母を充填層型反応
器に充填してビール等の酒類を製造する場合、発酵中に
産生する炭酸ガスのために以下に示す問題が生じる。 高レベルの溶存炭酸ガスが酵母の代謝生理に影響を及
ぼす。 炭酸ガスの滞留により死空間が形成され、固液接触面
積が減少する。 炭酸ガスによる圧力によってゲル粒子が変形し、粒子
同士の付着を促してガスや液の流路を塞ぎ、流れが不均
一となる。
2. Description of the Related Art In the process of producing liquor such as beer and wine, yeast generally consumes carbon and nitrogen sources in a brewing raw material liquid to produce ethyl alcohol. Technology for immobilizing yeast, for example, technology for embedding yeast in hydrous gel and immobilizing it has been developed, and then a method for producing beer by continuous brewing of wort has been proposed (J.Inst. Brew. , 84, 228 (1981) .Because yeast can be used at a high concentration, the brewing period can be greatly shortened.However, packed yeast is packed in a packed bed reactor and liquor such as beer is added. The following problems arise in the production of Lactobacillus due to the carbon dioxide produced during fermentation: High levels of dissolved carbon dioxide affect the metabolic physiology of yeasts. The contact area with liquid is reduced The gel particles are deformed by the pressure of carbon dioxide gas, which promotes the adhesion of particles to each other and blocks the flow paths of gas and liquid, resulting in non-uniform flow.

【0003】このような問題を解決するため、充填層型
反応器内に産生した炭酸ガスを加圧することにより液中
に溶解させる方法が試みられた(EBC Congress, Proc.,5
05(1981)) が、この方法では酵母の代謝生理への影響が
解消されない。ところで、発酵に用いるバイオリアクタ
ーは、攪拌槽型反応器,充填層型反応器および流
動層型反応器の3つの形式に大別されるが、これらはそ
れぞれ特有の長所と欠点を有している(バイオリアクタ
ーの合理的設計と最適操作、151(1986) 技術情報センタ
ー)。これら反応器のうち炭酸ガス排出効果の高いもの
は攪拌槽型反応器と流動層型反応器である。なかでも、
流動層型反応器は、温度やpHの制御が簡単で、物質の
移動特性が良く、固定化酵母の圧力損失が少ないという
特色があるため、アルコール発酵に用いられている。
In order to solve such a problem, a method of pressurizing carbon dioxide gas produced in a packed bed reactor to dissolve it in a liquid has been tried (EBC Congress, Proc., 5).
05 (1981)), but this method does not eliminate the effect on the metabolic physiology of yeast. By the way, the bioreactors used for fermentation are roughly classified into three types, that is, a stirred tank reactor, a packed bed reactor and a fluidized bed reactor, each of which has its own advantages and disadvantages. (Rational design and optimal operation of bioreactor, 151 (1986) Technical Information Center). Among these reactors, stirred tank type reactors and fluidized bed type reactors have a high carbon dioxide emission effect. Above all,
The fluidized bed reactor is used for alcohol fermentation because it is characterized by easy temperature and pH control, good mass transfer characteristics, and low pressure loss of immobilized yeast.

【0004】流動層型反応器を用いたアルコール発酵に
おいて、固定化酵母を流動させ、かつ炭酸ガスの排出を
よくするため、反応器の下部より不活性ガスを導入する
方法が提案されている(Chem. Eng. Sci.,19,215(1964))
が、ガスの回収等にコストがかかるため、実用的でな
い。また、機械的攪拌による方法は、固定化酵母が破壊
されるという致命的な欠点がある。さらに、充填層型反
応器に固定化酵母を充填して発酵を行った場合、酵母に
よる原料中のアミノ酸の取り込みが低く、得られる発酵
液のアミノ酸濃度が高くなり、香味上の問題がある。
In alcohol fermentation using a fluidized bed reactor, a method has been proposed in which an inert gas is introduced from the lower part of the reactor in order to fluidize the immobilized yeast and to improve the discharge of carbon dioxide gas ( Chem. Eng. Sci., 19,215 (1964))
However, it is not practical because it costs a lot to collect the gas. Further, the method using mechanical stirring has a fatal drawback that the immobilized yeast is destroyed. Furthermore, when the packed bed reactor is filled with immobilized yeast and fermentation is carried out, the incorporation of amino acids in the raw material by the yeast is low, the amino acid concentration of the resulting fermentation liquor is high, and there is a problem with flavor.

【0005】本発明の目的は、上記の諸問題を解決して
固定化酵母を用いる効率的な酒類の製造法を提供するこ
とである。本発明では、前記の反応器下部より不活性ガ
スを導入する方法の代わりに、液を循環させることによ
って固定化酵母を流動させる方法を採用している。
An object of the present invention is to solve the above problems and provide an efficient method for producing alcoholic beverages using immobilized yeast. In the present invention, instead of the method of introducing the inert gas from the lower part of the reactor, a method of circulating the liquid to flow the immobilized yeast is adopted.

【0006】[0006]

【課題を解決するための手段】本発明は、液循環用パイ
プとガス排気口を備えた流動層型反応器に固定化酵母を
充填し、該反応器に醸造原料液を供給し、反応器の上部
より培養液の一部を抜き出し、反応器の下部より反応器
内部に前記培養液を戻すことにより循環流を形成しつつ
培養することを特徴とする酒類の製造法である。さら
に、本発明は上記の方法による培養の途中で、反応器に
醸造原料液を供給すると共に、培養液の一部を反応器外
に抜き出すことにより連続的に酒類を製造する方法に関
する。
According to the present invention, a fluidized bed reactor equipped with a liquid circulation pipe and a gas exhaust port is filled with immobilized yeast, and the brewing raw material liquid is supplied to the reactor. The method for producing alcoholic beverages is characterized in that a part of the culture solution is withdrawn from the upper part of the above, and the culture solution is returned from the lower part of the reactor to the inside of the reactor to form a circulation flow for cultivation. Further, the present invention relates to a method for continuously producing liquor by supplying a brewing raw material liquid to a reactor and extracting a part of the culture liquid to the outside of the reactor during the culture by the above method.

【0007】本発明では、図1に示した流動層型反応器
を用いて酒類の製造を行う。この反応器では、発酵液の
一部を強制的に循環させることにより、産生した炭酸ガ
スの排出を容易にしている。具体的には、図示したよう
に、反応器内の発酵液を上部から抜き取りパイプを介し
て下部に導入することによって、発酵液を流動させてい
る。そのため、発酵中に産生した炭酸ガスは液に溶解す
ることなくガス排気口より反応器外に排出される。その
ため、炭酸ガスによる酵母の代謝活性への影響を回避す
ることができる。
In the present invention, liquor is produced using the fluidized bed reactor shown in FIG. In this reactor, a part of the fermentation broth is forcibly circulated to facilitate the discharge of the carbon dioxide gas produced. Specifically, as shown in the figure, the fermentation liquor in the reactor is drawn from the upper part and introduced into the lower part through a pipe to flow the fermentation liquor. Therefore, the carbon dioxide gas produced during fermentation is discharged from the reactor through the gas exhaust port without being dissolved in the liquid. Therefore, it is possible to avoid the influence of carbon dioxide on the metabolic activity of yeast.

【0008】醸造原料液としては、ビール酵母,ワイン
酵母,清酒酵母等の酒類酵母の増殖に適したものであれ
ばよく、既知のものを任意に使用することができるが、
通常は麦芽汁,果汁,糖液,穀類糖化液などが単独でも
しくは適宜混合して用いられる。その他、必要に応じて
適当な栄養分などを加えることができる。醸造原料液
は、常法により殺菌したのち固定化酵母の充填された流
動層型反応器に供給するが、その供給量は空間速度0.0
5〜0.2hr-1、好ましくは0.1〜0.2hr-1とする。
ここで、空間速度は流動層型反応器に供給される醸造原
料液の単位時間当たりの液量と酵母を担持した固定化担
体量とを乗算して求められるものである。なお、酵母を
担持した固定化担体の充填量は、反応器容積を基準とし
て5〜50容積%、好ましくは10〜30容積%が適当
である。また、醸造原料液は反応器の上部,下部などの
適当な位置から導入することができる。
As the brewing raw material liquid, any liquid suitable for the growth of liquor yeast such as brewer's yeast, wine yeast, sake yeast, etc. may be used, and any known liquid may be used.
Usually, wort, fruit juice, sugar solution, saccharified cereal solution, etc. are used alone or in an appropriate mixture. In addition, appropriate nutrients and the like can be added if necessary. The brewing raw material liquid is sterilized by a conventional method and then supplied to a fluidized bed reactor filled with immobilized yeast, and the supply amount thereof is space velocity 0.0.
It is set to 5 to 0.2 hr -1 , preferably 0.1 to 0.2 hr -1 .
Here, the space velocity is obtained by multiplying the liquid amount of the brewing raw material liquid supplied to the fluidized bed reactor per unit time by the amount of the immobilized carrier carrying yeast. The filling amount of the immobilized carrier carrying yeast is 5 to 50% by volume, preferably 10 to 30% by volume, based on the reactor volume. Further, the brewing raw material liquid can be introduced from an appropriate position such as the upper part or the lower part of the reactor.

【0009】次に、酒類の製造に用いる酵母としては、
醸造原料液を代謝してアルコールや炭酸ガス等を産生す
る、いわゆる酒類酵母が使用され、具体的にはサッカロ
ミセス・セレビシエ,サッカロミセス・ウバルム等を挙
げることができる。ビール酵母,ワイン酵母,清酒酵母
等の酒類酵母は、使用目的等に応じて適宜選択すればよ
く、例えばサッカロミセス・セレビシエOC−2,サッ
カロミセス・セレビシエKY−1,サッカロミセス・セ
レビシエKY−3,サッカロミセス・セレビシエKY−
4などがある。これら酵母は一般的によく知られてお
り、容易に入手することができる。
Next, as yeasts used for the production of alcoholic beverages,
So-called liquor yeast, which metabolizes the brewing raw material liquid to produce alcohol, carbon dioxide and the like, is used, and specific examples thereof include Saccharomyces cerevisiae and Saccharomyces ubalm. Alcoholic yeasts such as brewer's yeast, wine yeast and sake yeast may be appropriately selected depending on the purpose of use and the like. For example, Saccharomyces cerevisiae OC-2, Saccharomyces cerevisiae KY-1, Saccharomyces cerevisiae KY-3, Saccharomyces. Cerevisiae KY-
There are 4 etc. These yeasts are generally well known and can be easily obtained.

【0010】これら酵母は一般に通性嫌気性である。ま
た、酵母を担持するために用いる担体としては、各種の
ものが使用できるが、特にキトサンビーズ,アルギン酸
ビーズ,カラギーナンビーズ等が好適であり、セラミッ
クやガラスなどのビーズは磨耗に弱いので、本発明の担
体としては適当でない。なお、酵母の固定化について
は、それ自体公知であり、本発明においても公知の手法
により実施すればよい。
These yeasts are generally facultative anaerobic. Various carriers can be used as a carrier for supporting yeast, but chitosan beads, alginic acid beads, carrageenan beads and the like are particularly preferable, and beads such as ceramics and glass are weak against abrasion, and thus the present invention Is not suitable as a carrier. Immobilization of yeast is known per se, and the known method may be used in the present invention.

【0011】次に、発酵条件については基本的に既知の
条件と変わらない。発酵温度としては、例えばビール醸
造の場合は通常15℃以下、好ましくは8〜10℃であ
り、ワイン醸造の場合は通常20℃前後、好ましくは1
5〜20℃が適当である。また、発酵中に循環する発酵
液の循環速度は、例えば容量1リットルの反応器の場
合、1分間に150〜400ml、好ましくは200〜
250mlが適当である。このような条件下で発酵を行
うと、発酵液は完全混合に近い状態となり、効率よく発
酵を行うことができる。
Next, the fermentation conditions are basically the same as the known conditions. The fermentation temperature is, for example, usually 15 ° C or lower, preferably 8 to 10 ° C in the case of beer brewing, and is usually around 20 ° C, preferably 1 in the case of wine brewing.
5 to 20 ° C is suitable. Further, the circulation speed of the fermentation liquor circulated during fermentation is, for example, 150 to 400 ml, preferably 200 to 400 ml per minute in the case of a reactor having a volume of 1 liter.
250 ml is suitable. When fermentation is carried out under such conditions, the fermented liquid is in a state close to perfect mixing, and fermentation can be carried out efficiently.

【0012】本発明で用いる流動層型反応器は、前述し
たように、物質の移動特性が良好であるため、醸造原料
液に含まれるアミノ酸等は発酵過程において酵母に取り
込まれ、資化される。そのため、酒類製品中のアミノ酸
濃度は従来法によるものと比較して低減しており、香味
が良好である。本発明の方法は、ビールの製造の他にワ
イン,清酒などの他の酒類の製造にも利用できる。
As described above, since the fluidized bed reactor used in the present invention has good mass transfer characteristics, amino acids and the like contained in the brewing raw material liquid are taken up by yeast and assimilated in the fermentation process. . Therefore, the amino acid concentration in the liquor product is lower than that obtained by the conventional method, and the flavor is good. The method of the present invention can be used for the production of beer as well as other liquors such as wine and sake.

【0013】[0013]

【実施例】次に、本発明を実施例により説明する。 実施例1 ビール酵母(サッカロミセス・セレビシエIAM4206(ATCC
9080))を固定化した担体(キトサンビーズ)を容量1リ
ットルの流動層型反応器に250ml充填し、原麦汁エ
キス11%Plato に調整した麦汁を該反応器に750m
l導入し、反応器内発酵液の循環速度を250ml/分
に設定して11℃にて回分発酵を行った。
EXAMPLES The present invention will now be described with reference to examples. Example 1 Beer yeast (Saccharomyces cerevisiae IAM4206 (ATCC
9080))-immobilized carrier (chitosan beads) was filled in a fluidized bed reactor of 1 liter capacity in an amount of 250 ml, and wort adjusted to 11% Plato raw wort extract was placed in the reactor for 750 m.
1 was introduced, the circulation rate of the fermentation broth in the reactor was set to 250 ml / min, and batch fermentation was performed at 11 ° C.

【0014】反応器内発酵液の仮性エキスが2.5%Plat
o (発酵開始19時間後)になったところで、反応器下
部より麦汁を40ml/時間で通液し、反応器上部より
同量の発酵液を抜き出しながら、循環流の下で連続発酵
を開始した。その結果を図2に示す。図から明らかなよ
うに、発酵期間中の仮性エキスは2.5%Plato と安定し
ていた。また、発酵液中のアミノ酸濃度の測定値を第1
表に示した。本発明の方法によれば、酵母によりアミノ
酸が取り込まれ、資化されるため、発酵液中のアミノ酸
濃度は比較例や対照の方法に比べて低いことが判る。
2.5% Plating of the temporary extract of the fermentation liquid in the reactor
o When (19 hours after the start of fermentation), wort was passed through the lower part of the reactor at a rate of 40 ml / hour, and the same amount of fermented liquid was withdrawn from the upper part of the reactor, and continuous fermentation was started under a circulating flow. did. The result is shown in FIG. As is clear from the figure, the pseudo extract was stable at 2.5% Plato during the fermentation period. In addition, the measured value of the amino acid concentration in the fermentation broth is the first
Shown in the table. According to the method of the present invention, since the amino acid is taken up and assimilated by yeast, the amino acid concentration in the fermentation broth is lower than that of the comparative example or the control method.

【0015】[0015]

【表1】 [Table 1]

【0016】比較例1 容量500mlの充填型反応器を使用し、ビール酵母
(サッカロミセス・セレビシエIAM4206(ATCC9080))を固
定化したキトサンビーズ160mlを充填し、11℃で
発酵を行って、仮性エキス2.5%Plato の発酵液を得
た。この場合は、発酵中に産生した炭酸ガスが反応器内
に滞り、液の偏流が発生した。また、第1表に示したよ
うに、酵母によるアミノ酸の取り込みが不十分であるた
めに、発酵液中のアミノ酸濃度は高い。なお、固定化し
ないで遊離酵母を用いる従来の方法による発酵を行った
場合の発酵液(仮性エキス2.5%Plato)中のアミノ酸濃
度を参考のために示した。
Comparative Example 1 Using a packed reactor having a capacity of 500 ml, 160 ml of chitosan beads on which brewer's yeast (Saccharomyces cerevisiae IAM4206 (ATCC9080)) was immobilized was filled and fermented at 11 ° C. to obtain pseudo extract 2. A fermentation broth of 0.5% Plato was obtained. In this case, the carbon dioxide gas produced during fermentation stagnated in the reactor and liquid drift occurred. Further, as shown in Table 1, the amino acid concentration in the fermentation broth is high because the amino acid uptake by the yeast is insufficient. The amino acid concentration in the fermentation broth (pseudo extract 2.5% Plato) when fermentation was carried out by a conventional method using free yeast without immobilization is shown for reference.

【0017】実施例2 ワイン酵母(サッカロミセス・セルビシエOC−2、日
本醸造協会)を固定化した担体(キトサンビーズ)を容
量1リットルの流動層型反応器に250ml充填し、糖
度22%Plato に調整した麦汁を該反応器に750ml
導入し、反応器内発酵液の循環速度を250ml/分に
設定して20℃にて回分発酵を行った。
Example 2 A carrier (chitosan beads) on which wine yeast (Saccharomyces cerevisiae OC-2, Japan Brewing Society) was immobilized was filled in a fluidized bed reactor having a volume of 1 liter in an amount of 250 ml, and the sugar content was adjusted to 22% Plato. 750 ml of wort in the reactor
After the introduction, the circulation rate of the fermentation liquid in the reactor was set to 250 ml / min, and batch fermentation was performed at 20 ° C.

【0018】反応器内発酵液の仮性エキスが4.0%Plat
o (発酵開始40時間後)になったところで、反応器下
部よりブドウ果汁液を18ml/時間で通過し、反応器
上部より同量の発酵液を抜き出しながら、循環流の下で
連続発酵を開始した。その結果500時間にわたり安定
に発酵を行い、ワインを醸造することができた。
The temporary extract of the fermentation liquid in the reactor is 4.0% Plat
o When (40 hours after the start of fermentation), 18 ml / hour of grape juice was passed from the lower part of the reactor and the same amount of fermented liquid was withdrawn from the upper part of the reactor, and continuous fermentation was started under a circulating flow. did. As a result, it was possible to carry out stable fermentation for 500 hours to brew wine.

【0019】[0019]

【発明の効果】本発明によれば、酒類の製造に当たり、
固定化酵母を充填した流動層型反応器を用いると共に、
反応器内の発酵液を循環させることによって固定化酵母
を流動させるため、産生した炭酸ガスの大部分は液に溶
解することなく系外に排出することができる。しかも、
醸造原料液中のアミノ酸が効率よく酵母により資化され
るため、酒類製品中のアミノ酸濃度は従来法によるもの
と比較して低減しており、香味が良好である。
According to the present invention, when producing alcoholic beverages,
While using a fluidized bed reactor filled with immobilized yeast,
Since the immobilized yeast is made to flow by circulating the fermentation liquid in the reactor, most of the produced carbon dioxide gas can be discharged to the outside of the system without being dissolved in the liquid. Moreover,
Since the amino acid in the brewing raw material liquid is efficiently assimilated by yeast, the amino acid concentration in the alcoholic beverage product is lower than that in the conventional method, and the flavor is good.

【図面の簡単な説明】[Brief description of drawings]

【図1】 本発明に使用する流動層型反応器の1例を示
す説明図である。
FIG. 1 is an explanatory view showing an example of a fluidized bed reactor used in the present invention.

【図2】 実施例1の連続発酵中の仮性エキスの経時変
化を示すグラフである。
FIG. 2 is a graph showing the temporal change of the pseudo extract during continuous fermentation of Example 1.

【符号の説明】[Explanation of symbols]

(1)麦汁タンク (2)ポンプ (3)pHセンサー (4)流動層型反応器 (5)温度センサー (6)ガス排気口 (7)生成物タンク (1) Wort tank (2) Pump (3) pH sensor (4) Fluidized bed reactor (5) Temperature sensor (6) Gas exhaust port (7) Product tank

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 (C12C 11/00 C12R 1:865) (C12G 1/02 C12R 1:865) (C12N 1/18 C12R 1:865) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical indication (C12C 11/00 C12R 1: 865) (C12G 1/02 C12R 1: 865) (C12N 1/18 C12R 1: 865)

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 液循環用パイプとガス排気口を備えた流
動層型反応器に固定化酵母を充填し、該反応器に醸造原
料液を供給し、反応器の上部より培養液の一部を抜き出
し、反応器の下部より反応器内部に前記培養液を戻すこ
とにより循環流を形成しつつ培養することを特徴とする
酒類の製造法。
1. A fluidized bed reactor equipped with a liquid circulation pipe and a gas exhaust port is filled with immobilized yeast, the brewing raw material liquid is supplied to the reactor, and a part of the culture liquid is fed from the upper part of the reactor. Is extracted and the culture solution is returned from the lower part of the reactor to the inside of the reactor to carry out the culture while forming a circulation flow.
【請求項2】 請求項1記載の方法による培養の途中
で、反応器に醸造原料液を供給すると共に、培養液の一
部を反応器外に抜き出すことにより連続的に酒類を製造
する方法。
2. A method for continuously producing liquor by supplying a brewing raw material liquid to a reactor and withdrawing a part of the culture liquid out of the reactor during the culture according to the method of claim 1.
【請求項3】 反応器が、pHセンサーと温度センサー
を備えたものである請求項1記載の方法。
3. The method according to claim 1, wherein the reactor is equipped with a pH sensor and a temperature sensor.
【請求項4】 固定化酵母が、キトサン,アルギン酸お
よびカラギーナンの中から選ばれた担体に担持された酒
類酵母である請求項1記載の方法。
4. The method according to claim 1, wherein the immobilized yeast is liquor yeast supported on a carrier selected from chitosan, alginic acid and carrageenan.
JP34706793A 1993-09-07 1993-12-27 Alcohol production method Expired - Fee Related JP3604715B2 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
JP34706793A JP3604715B2 (en) 1993-09-07 1993-12-27 Alcohol production method
AU76236/94A AU674448B2 (en) 1993-09-07 1994-09-07 Method of producing liquor
CA002147511A CA2147511A1 (en) 1993-09-07 1994-09-07 Process for producing liquors
US08/424,433 US20010019731A1 (en) 1993-09-07 1994-09-07 Process for producing liquors
EP94926367A EP0669393A4 (en) 1993-09-07 1994-09-07 Method of producing liquor.
PCT/JP1994/001476 WO1995007343A1 (en) 1993-09-07 1994-09-07 Method of producing liquor
KR1019950701752A KR950704472A (en) 1993-09-07 1994-09-07 Recipe of Liquor
CN94190661A CN1068378C (en) 1993-09-07 1994-09-07 Method of producing liquor

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP5-246128 1993-09-07
JP24612893 1993-09-07
JP34706793A JP3604715B2 (en) 1993-09-07 1993-12-27 Alcohol production method

Publications (2)

Publication Number Publication Date
JPH07123969A true JPH07123969A (en) 1995-05-16
JP3604715B2 JP3604715B2 (en) 2004-12-22

Family

ID=26537576

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Country Status (8)

Country Link
US (1) US20010019731A1 (en)
EP (1) EP0669393A4 (en)
JP (1) JP3604715B2 (en)
KR (1) KR950704472A (en)
CN (1) CN1068378C (en)
AU (1) AU674448B2 (en)
CA (1) CA2147511A1 (en)
WO (1) WO1995007343A1 (en)

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JP2016503652A (en) * 2012-12-31 2016-02-08 トランス バイオ − ディーゼル リミテッド Enzymatic transesterification / esterification treatment system and process using hydrophobic resin-immobilized lipase
JP2016152781A (en) * 2015-02-20 2016-08-25 サッポロビール株式会社 Method for producing beer taste beverage, and beer taste beverage
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Also Published As

Publication number Publication date
EP0669393A4 (en) 1996-03-06
WO1995007343A1 (en) 1995-03-16
AU674448B2 (en) 1996-12-19
US20010019731A1 (en) 2001-09-06
AU7623694A (en) 1995-03-27
CA2147511A1 (en) 1995-03-16
CN1114111A (en) 1995-12-27
CN1068378C (en) 2001-07-11
JP3604715B2 (en) 2004-12-22
EP0669393A1 (en) 1995-08-30
KR950704472A (en) 1995-11-20

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